Technical Field
[0001] The present invention relates to a catheter to be inserted into a biological lumen.
Background Art
[0002] A treatment catheter is widely used for diagnosis or treatment in a biological lumen.
The treatment catheter includes, for example, a balloon catheter used for percutaneous
transluminal coronary angioplasty (PTCA).
[0003] A guiding catheter is inserted into the biological lumen in advance before the treatment
catheter is inserted. The treatment catheter is inserted through a lumen of the guiding
catheter. Recently, a technique (TRI: Trans Radial Intervention) is increasing in
which the guiding catheter is inserted through an artery of an arm, particularly through
a radial artery or brachial artery in the treatment of blood vessels of lower extremity.
[0004] Since an elongated shaft of the guiding catheter used for TRI technique needs to
be inserted into a radial artery having a small diameter, the outer diameter of the
shaft needs to be as small as possible. On one hand, in order to insert the treatment
catheter through the lumen of the guiding catheter, the inner diameter of the shaft
needs to be as large as possible. Therefore, a wall thickness of the shaft of the
guiding catheter used for TRI technique needs to be small.
[0005] In the catheter, a reinforcement body may be provided in the shaft in order to secure
sufficient strength even if the wall thickness of the shaft is small. Generally, the
reinforcement body is generally a product obtained by weaving metallic wires. Examples
of the catheter having a reinforcement body are, for example, disclosed in PTL 1.
Citation List
Patent Literature
Summary of Invention
Technical Problem
[0007] Generally, when the wall thickness of the shaft is reduced, breaking strength against
tensile load of the shaft is reduced. In a case of the shaft having a reinforcement
body, breaking tends to occur in the end portion of the reinforcement body. It is
because the wall thickness of the shaft is the thinnest in the end portion of the
reinforcement body, so that the shaft tends to be the starting point of elongation
caused by tension, and the stress concentrates. Moreover, the presence of an edge
in the end portion of the reinforcement body is also cited as a reason that the shaft
tends to be the starting point of the breaking.
[0008] Therefore, even if the wall thickness of the shaft is small, a distal end portion
of the shaft including the end portion of the reinforcement body is required to have
high breaking strength.
[0009] The present invention has been made to solve the above-described problems, and an
object of the present invention is to provide a catheter having a distal end portion
of a shaft with high breaking strength even if the wall thickness thereof is small.
Solution to Problem
[0010] A catheter according to the present invention that achieves the above-described object
is the catheter including an elongated tube shaped shaft, in which the shaft has an
inner layer having a lumen along a length direction, an outer layer covering an outer
peripheral side of the inner layer, and a reinforcement body disposed on the outer
peripheral side of the inner layer, the outer layer has a distal outer layer of a
distal end portion of the shaft, an intermediate outer layer more proximal than the
distal outer layer, and a base outer layer more proximal than the intermediate outer
layer, and the intermediate outer layer is more flexible and thicker than the base
outer layer, and a distal end of the reinforcement body is located more proximal than
a distal end of the intermediate outer layer.
Advantageous Effects of Invention
[0011] With the catheter configured as described above, it is possible to increase the breaking
strength of the distal end portion of the flexible shaft while suppressing the occurrence
of the stress concentration in the distal end of the reinforcement body when the shaft
is pulled.
[0012] The reinforcement body includes metallic wires woven into a mesh shape, and distal
end portions of the wires located at the distal end of the reinforcement body have
a curved shape having no corner portion. Accordingly, it is possible to further reduce
the stress concentration when the shaft is pulled at the distal end of the reinforcement
body.
[0013] In the distal end portion of the reinforcement body, an intersection portion in which
the wires overlap each other is disposed, and the wires overlapping each other in
the intersection portion are fixed. Accordingly, it is possible to prevent the distal
ends of the wires from breaking through the intermediate outer layer when the shaft
is pulled.
[0014] In the reinforcement body, metallic wires are embedded inside the outer layer, and
the ratio of the thickness of the intermediate outer layer to twice the thickness
of the wires is within the range of 1.8 to 2.4. Accordingly, it is possible to prevent
increase in the outer diameter of the shaft and the maneuverability in the blood vessel
from being deteriorated while securing the thickness of the intermediate outer layer.
[0015] The distance between a distal end position of the intermediate outer layer and a
distal end position of the reinforcement body is within the range of 1.0 to 2.0 mm.
Accordingly, when the shaft is pulled, it is possible to suppress the deterioration
in the pushability of the shaft while sufficiently securing the elongation length
of the intermediate outer layer.
[0016] The reinforcement body includes metallic wires woven at regular pitches into a mesh
shape, and the distance between the distal end position of the intermediate outer
layer and the distal end position of the reinforcement body is within the range of
three to seven times the pitch of the reinforcement body. Accordingly, the length
of the portion not having the reinforcement body of the intermediate outer layer can
be set within the appropriate range.
Brief Description of Drawings
[0017]
Fig. 1 is a front view of a catheter of a present embodiment.
Fig. 2 is a cross-sectional view of a distal end portion of a shaft.
Fig. 3 is a partial front view of a reinforcement body.
Fig. 4 is a partial enlarged front view of a distal end portion of the reinforcement
body.
Fig. 5 is a partial enlarged front view of the reinforcement body in a state before
a wire is cut.
Fig. 6 is a cross-sectional view of the shaft in a region of an intermediate outer
layer.
Fig. 7 is a graph showing a relationship between a breaking elongation length λ and
a wall thickness ratio r.
Fig 8 is a graph showing a relationship between the breaking elongation length λ and
a length L of a distal side portion.
Description of Embodiments
[0018] Hereinafter, an embodiment of the present invention will be described with reference
to the drawings. Note that, for the convenience of description, there are cases where
the dimensional ratios of the drawings are exaggerated and are different from the
actual ratios. Note that, in the present specification, a side in which a catheter
10 is inserted into a biological lumen is referred to as a "distal end" or a "distal
side", and a hand-side to be operated is referred to as a "proximal end" or a "proximal
side".
[0019] The catheter 1 of the present embodiment is a guiding catheter inserted from a blood
vessel of an arm such as a radial artery to a vicinity of a target site such as a
stenosed site of the blood vessel of a lower extremity. The guiding catheter is used
to introduce a treatment catheter such as a balloon catheter to a target site by inserting
the treatment catheter inside thereof. As shown in Fig 1, the catheter 1 has a shaft
2 which is an elongated tube shaped body and a hub 3 provided in a proximal end portion
of the shaft 2.
[0020] As shown in Fig. 2, the shaft 2 is a tube shaped body having a two-layer structure
of an inner layer 10 having a lumen 11 along a length direction and an outer layer
12 covering an outer peripheral side of the inner layer 10. Moreover, the shaft 2
has a reinforcement body 13 between the inner layer 10 and the outer layer 12. The
shaft 2 is formed of a flexible material. Therefore, the shaft 2 can be inserted along
the shape of the blood vessel.
[0021] Examples of the material of the outer layer 12 include thermoplastic elastomers such
as a styrene-based elastomer, a polyolefin-based elastomer, a polyurethane-based elastomer,
a polyester-based elastomer, a polyamide-based elastomer, a polybutadiene-based elastomer,
a trans-polyisoprene-based elastomer, a fluororubber-based elastomer, and a chlorinated
polyethylene-based elastomer. One type or a combination of two or more types of these
materials (polymer alloy, polymer blend, laminated body, and the like) can be used
as the material of the outer layer 12.
[0022] It is desirable that the inner layer 10 is made of a material which has low friction
in a portion contacting a medical instrument when the medical instrument such as the
treatment catheter is inserted into the lumen 11. Accordingly, the medical instrument
inserted into the shaft 2 can be moved in the length direction against smaller sliding
friction, thereby improving operability. Examples of a low-friction material include
a fluorine-based resin such as polytetrafluoroethylene (PTFE).
[0023] The reinforcement body 13 is provided to reinforce the shaft 2. As shown in Fig.
3, the reinforcement body 13 includes a plurality of wires 30 woven at regular pitches
P into a mesh shape. Here, the pitch P refers to an axial distance between intersection
portions 31 where the wires 30 intersect each other. A resin material of the outer
layer 12 enters a gap between the plurality of wires 30 of the reinforcement body
13. The material of the wire 30 is a metal such as stainless steel or NiTi. The cross-sectional
shape of the wire 30 is formed in a flat plate shape. Accordingly, it is possible
to reduce the thickness of the reinforcement body 13. However, the cross-sectional
shape of the wire 30 is not limited to this, and may be circular, elliptical, oval,
or polygonal or the like. Moreover, the wire 30 may be made of a resin material.
[0024] The outer layer 12 is further separated into three portions in the length direction
of the shaft 2. The distal end portion of the shaft 2 is a distal outer layer 20.
An intermediate outer layer 21 is provided more proximal than the distal outer layer
20. A proximal outer layer 22 is provided more proximal than the intermediate outer
layer 21. The intermediate outer layer 21 is formed of a material having more flexibility
than the proximal outer layer 22. Moreover, the distal outer layer 20 is formed of
a material having more flexibility than the intermediate outer layer 21. The hardness
of the proximal outer layer 22 is within the range of the shore D hardness 50 to 80,
and more preferably in the range of the shore D hardness 60 to 70. The hardness of
the intermediate outer layer 21 is within the range of the shore D hardness 35 to
50, and more preferably within the range of the shore D hardness 45 to 50. The hardness
of the distal outer layer 20 is within the range of the shore D hardness 30 to 50,
and more preferably within the range of the shore D hardness 40 to 45.
[0025] In the outer layer 12, the intermediate outer layer 21 and the distal outer layer
20 are thicker than the proximal outer layer 22. In the region of the intermediate
outer layer 21 and the distal outer layer 20, the cross-sectional area of the shaft
2 is constant along the length direction.
[0026] The distal outer layer 20 contains a substance having an X-ray radiopacity. On the
other hand, the intermediate outer layer 21 does not have a radiopacity. Therefore,
when the shaft 2 is inserted into the blood vessel, only the distal end portion of
the shaft 2 can be imaged under the X-ray fluoroscopy to improve visibility.
[0027] The reinforcement body 13 is provided over from the proximal outer layer 22 to the
intermediate outer layer 21 in the length direction of the shaft 2. Moreover, the
distal end of the reinforcement body 13 is located more proximal than the distal end
of the intermediate outer layer 21. Therefore, the intermediate outer layer 21 has
a proximal side portion 21a which has the reinforcement body 13 and a distal side
portion 21b which does not have the reinforcement body 13.
[0028] As shown in Fig. 4, the intersection portion 31 of wires 30 is disposed in the distal
end portion of the reinforcement body 13. The intersection portion 31 has weld portions
35 in a portion which becomes both sides of the distal end portion of each of the
two wires 30 overlapping each other. The two wires 30 overlapping each other in the
intersection portion 31 of the distal end portion of the reinforcement body 13 are
welded and bonded in the weld portions 35. In the weld portions 35 located at the
distal ends of the intersection portion 31, the wires 30 have a curved shape having
no corner in the end portion. The curved shape is formed when the wires 30 are bonded
to each other.
[0029] The distal end shape of the reinforcement body 13 shown in Fig. 4 is formed as follows.
As shown in Fig. 5, in the intersection portion 31 where two wires 30 are overlapping
each other, each of the wires 30 is laser cut at a first line 37 and a second line
38 respectively along the side of the other wire 30. At the same time, the wires 30
are welded and bonded to each other by laser welding at the first line 37 and the
second line 38. At this time, a curved shape located at the distal end of the intersection
portion 31 is formed. Moreover, a bulge shape is formed on a surface of the welded
portion of the intersection portion 31.
[0030] Note that, as a method of bonding the wires 30 to each other, other methods such
as resistance welding, soldering, brazing, or adhesion with an adhesive may be used
in addition to the laser welding.
[0031] If the shaft 2 is pulled in the proximal direction in a case where the distal end
portion of the shaft 2 in the blood vessel is moored or during the operation of removing
the shaft 2 from the blood vessel, the shaft 2 is elongated by the tensile load. As
described above, the intermediate outer layer 21 is flexible, and the proximal outer
layer 22 has flexibility lower than the intermediate outer layer 21. Therefore, when
elongating the shaft 2, first, a portion of the intermediate outer layer 21 which
has high flexibility and small yield point load is elongated. Next, a portion of the
proximal outer layer 22 is elongated.
[0032] When the portion of the proximal outer layer 22 starts to be elongated, the tensile
load applied to the distal end portion of the shaft 2 increases. When the tensile
load is increased, the breaking occurs in the region of the intermediate outer layer
21. In the present embodiment, the intermediate outer layer 21 is thicker than the
proximal outer layer 22 in the shaft 2, so that the breaking strength against the
tensile load of the shaft 2 can be increased.
[0033] The intersection portion 31 is disposed as described above in the distal end portion
of the reinforcement body 13. When bonding the wires 30 in the intersection portion
31 together, a bulge shape is formed in the intersection portion 31, and the wall
thickness is larger than other portions. In contrast, when the intermediate outer
layer 21 is thicker than the proximal outer layer 22, it is possible to prevent the
distal end portion of the reinforcement body 13 from being exposed on the outer surface
of the intermediate outer layer 21. When the reinforcement body 13 is exposed on the
outer surface of the intermediate outer layer 21, stress concentration occurs in that
portion during pulling of the shaft 2, and thereby the breaking strength of the shaft
2 is reduced. Since this is prevented in the present embodiment, the breaking strength
against the tensile load of the shaft 2 can be increased. A certain thickness is required
between a bulge shaped surface of the reinforcement body 13 and a surface of the intermediate
outer layer 21. On the other hand, when the thickness of the intermediate outer layer
21 is too thick, the outer diameter of the shaft 2 is increased so that the maneuverability
in the blood vessel is reduced. Therefore, the thickness of the intermediate outer
layer 21 is required to be set within an appropriate range. The appropriate thickness
range of the intermediate outer layer 21 will be described later.
[0034] In a case where the shaft 2 is pulled, the stress concentration occurs at the distal
end of the reinforcement body 13, so that the breaking tends to occur in this position.
If the reinforcement body 13 is provided up to the distal end of the intermediate
outer layer 21, the stress concentration occurs at the vicinity of the boundary between
the intermediate outer layer 21 and the distal outer layer 22, so that it tends to
break more easily. In the present embodiment, the distal end of the reinforcement
body 13 is located more proximal than the distal end of the intermediate outer layer
21. That is, since the intermediate outer layer 21 has the distal side portion 21b
which does not have the reinforcement body 13, this problem can be suppressed.
[0035] When the intermediate outer layer 21 does not have the distal side portion 21b or
the distal side portion 21b thereof is too short, the yield elongation length in the
portion of the intermediate outer layer 21 is reduced when the shaft 2 is pulled.
In this case, the elongation of the portion of the proximal outer layer 22 starts
early, and the tensile load applied to the distal end portion of the reinforcement
body 13 increases early. Therefore, the shaft 2 tends to break in a position at the
vicinity of the distal end portion of the reinforcement body 13. In contrast, when
the distal side portion 21b is provided with a length equal to or more than a certain
length, the yield elongation length of the portion of the intermediate outer layer
21 increases, so that this problem can be suppressed. On the other hand, when the
length of the distal side portion 21b is too long, the length of the portion which
does not have the reinforcement body 13 increases in the distal end portion of the
shaft 2. For this, the pushability of the shaft 2 is reduced, and the operability
of the catheter 1 is reduced. Therefore, the length of the distal side portion 21b
is required to be set within an appropriate range. The appropriate range of the length
of the distal side portion 21b will be described later.
[0036] Moreover, by providing the distal side portion 21b which does not have the reinforcement
body 13 in the intermediate outer layer 21, the sliding friction of the medical instrument
passing through the lumen 11 of the shaft 2 is reduced. In the TRI technique, an operator
inserts a balloon catheter into the lumen 11 of the shaft 2, and inflates the balloon
at a target site in the blood vessel. Thereafter, the operator deflates the balloon
to remove the balloon catheter through the shaft 2. At the time of removal, the outer
diameter of the balloon is slightly larger than at the time of insertion. Therefore,
at the time of removing the balloon catheter, the sliding friction of the balloon
against the distal end portion of the shaft 2 increases. Since the catheter 1 of the
present embodiment has the distal side portion 21b which does not have the reinforcement
body 13 in the intermediate outer layer 21, when the balloon passes through the distal
end portion of the shaft 2, the distal side portion 21b tends to be widened in the
circumferential direction. Therefore, with the catheter 1 of the present embodiment,
the sliding friction at the time of removing the balloon catheter can be reduced.
[0037] Moreover, in the catheter 1 of the present embodiment, since the intermediate outer
layer 21 has the distal side portion 21b which does not have the reinforcement body
13, the distance from the distal end of the shaft 2 to the distal end of the reinforcement
body 13 is large. Therefore, the spread of the inner diameter from the proximal side
of the shaft 2 toward the distal side is milder compared to the case where the distal
end of the reinforcement body 13 is located near the distal end portion of the shaft
2. Therefore, the catheter 1 of the present embodiment can reduce the load against
the distal end portion of the shaft 2 and the distal end portion of the reinforcement
body 13.
[0038] When a single wire 30 is disposed in the end portion of the reinforcement body 13,
the wire 30 tends to break through the intermediate outer layer 21 and to be exposed
on the outer surface of the shaft 2. In the catheter 1 of the present embodiment,
the intersection portion 31 in which the wires 30 are bonded to each other is disposed
in the distal end portion of the reinforcement body 13, so that the possibility can
be reduced. Moreover, since the distal end of the intersection portion 31 is formed
into a curved shape having no corner, when the tensile load is applied to the shaft
2, the stress concentration at the distal end of the reinforcement body 13 is relieved,
and the breaking of the shaft 2 can be suppressed.
[0039] Moreover, the wires 30 forming the reinforcement body 13 are fixed only in the intersection
portion 31 of the distal end portion. Such a reinforcement body 13 is more likely
to be elastically deformed also on the side more proximal than the distal end portion
as compared to the case where the wires 30 are fixed to each other. Therefore, when
a site having a large outer diameter such as the balloon after being inflated and
deflated once passes through the inside of the shaft 2 in the medical instrument,
the inner diameter tends to spread in the distal end portion of the shaft 2, and the
maneuverability of the medical instrument can be improved.
[0040] The catheter 1 of the present embodiment has the inner layer 10 which is continuous
over the proximal outer layer 22, the intermediate outer layer 21, and the distal
outer layer 20. Therefore, at the time of removing a medical instrument such as a
balloon catheter, it is possible to prevent the distal end portion of the shaft 2
from being caught in the lumen 11 of the shaft 2 by reducing the sliding friction
of the distal end portion of the shaft 2.
[0041] In the present embodiment, the wall thickness of the distal outer layer 20 is the
same as that of the intermediate outer layer 21. Therefore, the distal outer layer
20 is thick-walled so that it prevents the distal end portion of the shaft 2 from
being caught in the lumen 11 of the shaft 2. The wall thickness of the distal outer
layer 20 may be smaller or larger than the wall thickness of the intermediate outer
layer 21, but it is desirable to be thick-walled as in the present embodiment.
[0042] As shown in Fig. 6, the wall thickness of the shaft 2 in the portion of the intermediate
outer layer 21, the wall thickness of the inner layer 10, and the wall thickness of
the intermediate outer layer 21 are referred to as T0, T1, and T2, respectively. Moreover,
the thickness of the portion where the wires 30 of the reinforcement body 13 are overlapped
is referred to as t. The portion where the wires 30 of the reinforcement body 13 are
overlapped is the intersection portion 31 where the wires 30 intersects in Fig. 3.
The ratio T2/t of the wall the thickness T2 of the intermediate outer layer 21 to
the thickness t of the reinforcement body 13 is referred to as a wall thickness ratio
r. Moreover, the axial length of the distal side portion 21b which does not have the
reinforcement body 13 of the intermediate outer layer 21 is referred to as L.
[0043] The applicant manufactured a plurality of shafts 2 having different wall thicknesses
of the intermediate outer layer 21, and measured the tensile strength and breaking
elongation length λ thereof. Three kinds of shafts 2 having different wall thicknesses
of the intermediate outer layer 21 were prepared. The conditions of the inner diameter
and the wall thickness T1 of the inner layer 10 of each of the shafts 2 are the same.
Moreover, in the shafts 2, the outer diameter of the region of the proximal outer
layer 22 is 2.37 mm. The dimensions and measurement results of the shafts 2 of the
conditions are shown in Table 1, and the relationship between the breaking elongation
length λ and the wall thickness ratio r is shown in Fig. 7, respectively.
[Table 1]
| |
Condition 1-1 |
Condition 1-2 |
Condition 1-3 |
| Outer diameter (mm) |
2.39 |
2.40 |
2.43 |
| Inner diameter (mm) |
2.20 |
2.20 |
2.20 |
| Shaft wall thickness T0 (mm) |
0.095 |
0.100 |
0.115 |
| Inner layer wall thickness T1 (mm) |
0.01 |
0.01 |
0.01 |
| Intermediate outer layer wall thickness T2 (mm) |
0.085 |
0.090 |
0.105 |
| Reinforcement body thickness t (mm) |
0.050 |
0.050 |
0.050 |
| Wall thickness ratio r |
1.7 |
1.8 |
2.1 |
| Tensile strength (gf) |
980 |
1191 |
1292 |
| Breaking elongation length (mm) |
17.0 |
19.6 |
36.0 |
[0044] According to the result, it is found that the larger the wall thickness ratio r,
which is the ratio of the wall the thickness T2 of the intermediate outer layer 21
to the thickness t of the reinforcement body 13, the greater tensile strength and
breaking elongation length. Since the tensile strength of the shaft 2 is required
to be 1,000 gf or more, Condition 1-1 does not satisfy the requirement. Therefore,
the lower limit value of the wall thickness ratio r is 1.8. In a case where the wall
thickness ratio r is larger than 2.4, the outer diameter of the shaft 2 is larger
than 2.46 mm. In this case, it exceeds the maximum value of the required outer diameter,
and the distal end portion of the shaft 2 becomes hard so that the operability of
the catheter 1 is deteriorated. Therefore, the upper limit value of the wall thickness
ratio r is 2.4. From the above, it is preferable that the wall thickness ratio r set
within the range of 1.8 to 2.4.
[0045] The thickness obtained by subtracting the thickness t of the reinforcement body 13
from the wall thickness T2 of the intermediate outer layer 21 corresponds to the thickness
between the surface of the reinforcement body 13 and the surface of the shaft 2. When
the range of the wall thickness ratio r is 1.8 to 2.4, the thickness between the surface
of the reinforcement body 13 and the surface of the shaft 2 is 0.04 to 0.07 mm. The
thickness needs to be 0.02 mm or more. In the intersection portion 31 disposed at
the distal end of the reinforcement body 13, a bulge shape by bonding is formed as
described above. Even in the consideration of the height of the bulge shape, if the
wall thickness ratio r is set within the range of 1.8 to 2.4, it is possible to secure
the thickness between the surface of the reinforcement body 13 and the surface of
the shaft 2 to be 0.02 mm or more.
[0046] Moreover, the applicant manufactured a plurality of shafts 2 having different lengths
L of the distal side portion 21b, and measured the tensile strength and the breaking
elongation length λ thereof. Three kinds of shafts 2 having different lengths L of
the distal side portion 21b were prepared. The conditions of the outer diameter, the
inner diameter, and the inner layer wall thickness of each of the shafts 2 are the
same. Moreover, in the shafts 2, the outer diameter of the region of the proximal
outer layer 22 is 2.37 mm. The dimensions and measurement results of the shafts 2
of the conditions are shown in Table 2, and the relationship between the breaking
elongation length λ and the length L of the distal side portion 21b is shown in Fig.
8, respectively. Note that, Condition 2-2 is under the same condition as Condition
1-3.
[Table 2]
| |
Condition 2-1 |
Condition 2-2 |
Condition 2-3 |
| Outer diameter (mm) |
2.43 |
2.43 |
2.43 |
| Inner diameter (mm) |
2.20 |
2.20 |
2.20 |
| Shaft wall thickness T0 (mm) |
0.115 |
0.115 |
0.115 |
| Inner layer wall thickness T1 (mm) |
0.01 |
0.01 |
0.01 |
| Intermediate outer layer wall thickness T2 (mm) |
0.105 |
0.105 |
0.105 |
| Reinforcement body thickness t (mm) |
0.050 |
0.050 |
0.050 |
| Distal side portion length L (mm) |
0.5 |
1.0 |
2.0 |
| Tensile strength (gf) |
910 |
1292 |
1288 |
| Breaking elongation length (mm) |
3.58 |
36.0 |
39.0 |
[0047] According to the result, the length L of the distal side portion 21b is desirable
to be within the range of 1.0 to 2.0 mm. Moreover, the pitch P of the reinforcement
body 13 is within the range of 0.27 to 0.42 mm. Therefore, the length L of the distal
side portion 21b is set within the range of three to seven times the pitch P of the
reinforcement body 13, more preferably to the range of three to five times.
[0048] As described above, the catheter 1 according to the present embodiment includes the
elongated tube shaped shaft 2. The shaft 2 has the inner layer 10 having the lumen
11 along the length direction, the outer layer 12 covering the outer peripheral side
of the inner layer 10, and the reinforcement body 13 disposed on the outer peripheral
side of the inner layer 10. The outer layer 12 has the distal outer layer 20 of the
distal end portion of the shaft 2, the intermediate outer layer 21 more proximal than
the distal outer layer 20, and the base outer layer 22 more proximal than the intermediate
outer layer 21. The intermediate outer layer 21 is more flexible and thicker than
the base outer layer 22, and the distal end of the reinforcement body 13 is located
more proximal than the distal end of the intermediate outer layer 21. With the catheter
1, it is possible to increase the breaking strength of the distal end portion of the
flexible shaft 2 while suppressing the occurrence of the stress concentration at the
distal end of the reinforcement body 13 when the shaft 2 is pulled.
[0049] Moreover, the reinforcement body 13 includes metallic wires 30 woven into a mesh
shape, and the distal end portions of the wires 30 located at the distal end of the
reinforcement body 13 have a curved shape having no corner portion. Accordingly, it
is possible to further reduce the stress concentration when the shaft 2 is pulled
at the distal end of the reinforcement body 13.
[0050] Moreover, in the distal end portion of the reinforcement body 13, the intersection
portion 31 in which the wires 30 overlap each other is disposed, and the wires 30
overlapping each other in the intersection portion 31 are fixed. Accordingly, it is
possible to prevent the distal ends of the wires 30 from breaking through the intermediate
outer layer 21 when the shaft 2 is pulled.
[0051] Moreover, in the reinforcement body 13, the metallic wires 30 are embedded inside
the outer layer 12, and the ratio of the thickness of the intermediate outer layer
21 to twice the thickness of the wires 30 is within the range of 1.8 to 2.4. Accordingly,
it is possible to prevent the increase in the outer diameter of the shaft 2 and the
maneuverability in the blood vessel from being deteriorated while securing the thickness
of the intermediate outer layer 21.
[0052] Moreover, the distance between the distal end position of the intermediate outer
layer 21 and the distal end position of the reinforcement body 13 is within the range
of 1.0 to 2.0 mm. Accordingly, when the shaft 2 is pulled, it is possible to suppress
the deterioration in the pushability of the shaft 2 while sufficiently securing the
elongation length of the intermediate outer layer 21.
[0053] Moreover, the reinforcement body 13 includes metallic wires 30 woven at regular pitches
into a mesh shape, and the distance between the distal end position of the intermediate
outer layer 21 and the distal end position of the reinforcement body 13 is within
the range of three to seven times the pitch of the reinforcement body 13. Accordingly,
the length of the portion not having the reinforcement body 13 of the intermediate
outer layer 21 can be set within the appropriate range.
[0054] Note that, the present invention is not limited to the embodiments described above,
and various changes can be made by those skilled in the art within the technical scope
and gist of the catheter and method disclosed here.
Reference Signs List
[0056]
- 1
- catheter
- 2
- shaft
- 3
- hub
- 10
- inner layer
- 11
- lumen
- 12
- outer layer
- 13
- reinforcement body
- 20
- distal outer layer
- 21
- intermediate outer layer
- 21a
- proximal side portion
- 21b
- distal side portion
- 22
- proximal outer layer
- 30
- wire
- 31
- intersection portion
- 35
- weld portion
- 36
- weld point
- 37
- first line
- 38
- second line